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PedAM

Pediatric Disease Annotations & Medicines




Disease alport syndrome
Phenotype C0035078|renal failure
Sentences 4
PubMedID- 20221644 A 61-year-old woman with chronic renal failure (crf) associated with alport syndrome underwent coronary artery aneurysmectomy under general anesthesia.
PubMedID- 20428923 In addition, α3(iv), α4(iv) or α5(iv) mutations cause alport syndrome, which leads to renal failure, deafness and retinopathy in patients [27, 88, 89].
PubMedID- 25165179 The hereditary type iv collagen disease alport syndrome (as) always leads to end-stage renal failure.
PubMedID- 25649157 Lenticonus and central fleck retinopathy strongly suggest the diagnosis of alport syndrome and are associated with renal failure before the age of 30 years, in males with x-linked disease.

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